ISO/TC 212

Reģistrācijas numurs (WIID)Projekta Nr.NosaukumsStatuss
51984ISO 19001:2013In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyStandarts spēkā
87738ISO 22367:2026Laboratoires de biologie médicale — Application de la gestion des risques aux laboratoires de biologie médicaleStandarts spēkā
42022ISO 15194:2009In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for certified reference materials and the content of supporting documentationStandarts spēkā
69802ISO 20166-2:2018Analyses de diagnostic moléculaire in vitro — Spécifications relatives aux processus préanalytiques pour les tissus fixés au formol et inclus en paraffine (FFPE) — Partie 2: Protéines extraitesStandarts spēkā
67217ISO 20186-1:2019Analyses de diagnostic moléculaire in vitro — Spécifications relatives aux processus préanalytiques pour le sang total veineux — Partie 1: ARN cellulaire extraitStandarts spēkā
77070ISO/TS 23824:2024Medical laboratories — Guidance on application of ISO 15189 in anatomic pathologyStandarts spēkā
72191ISO 15190:2020Laboratoires de biologie médicale — Exigences pour la sécuritéStandarts spēkā
67215ISO 20184-1:2018Analyses de diagnostic moléculaire in vitro — Spécifications relatives aux processus préanalytiques pour les tissus congelés — Partie 1: ARN extraitStandarts spēkā
70960ISO 21474-1:2020In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 1: Terminology and general requirements for nucleic acid quality evaluationStandarts spēkā
85349ISO 18704:2026Molecular in vitro diagnostic examinations — Requirements and recommendations for pre-examination processes for urine and other body fluids — Isolated cell-free DNAStandarts spēkā
Attēlo no 111. līdz 120. no pavisam 146 ieraksta(-iem).